| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3079569 | Neuromuscular Disorders | 2011 | 4 Pages |
Abstract
We describe a patient with this uncommon myopathy, caused by a new p.K1784delK mutation in the MYH7 gene. The patient developed a severe thoracolumbar scoliosis and had scoliosis surgery.
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Authors
Xenia Stalpers, Aad Verrips, Jan Braakhekke, Martin Lammens, Arthur van den Wijngaard, Adriaan Mostert,